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Clinical Trial Summary

To evaluate the efficacy and safety of 26-weeks of treatment with riociguat vs. placebo in patients with symptomatic PH (pulmonary hypertension) associated with IIP (idiopathic interstitial pneumonias).


Clinical Trial Description

Number of participants with Adverse Events (AEs) will be reported in Adverse Events section. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02138825
Study type Interventional
Source Bayer
Contact
Status Terminated
Phase Phase 2
Start date June 4, 2014
Completion date September 14, 2016